Local woman recovering from Guillain-Barré shares life-saving advice

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  • čas přidán 27. 08. 2024
  • Just one week after getting the COVID-19 vaccine, an Indiana woman says she could barely walk or talk. The sad part, she says, is her illness might have been avoided if she simply knew to have an important conversation with her doctor first: bit.ly/3sa7kgP
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Komentáře • 17

  • @sandrasmith9331
    @sandrasmith9331 Před 2 lety +8

    I had guillain barre 17 yrs ago and my doctor told me never to get the flu vaccine and now he told me to wait on getting the Covid-19 vaccine. Thank you so much for sharing your story

  • @woodman2182
    @woodman2182 Před rokem +5

    I was diagnosed with Guillain-barre in January of 2022 and still recovering

    • @johnhironimus5748
      @johnhironimus5748 Před 10 měsíci

      God speed your healing i too share this journey have had this since may 17 hope your healing well and praying for your recovery

  • @laurengrant7722
    @laurengrant7722 Před rokem +4

    I myself had guillain barre syndrome from the covid 19 vaccine I had guillain barre syndrome about 2 years this year so I'm still In recovery i can walk but I can't walk far distance and my balance is still poor

  • @sheiladraper2682
    @sheiladraper2682 Před 11 měsíci +2

    My daughter got GBS and she is better!!

  • @phil_pykles
    @phil_pykles Před 5 měsíci

    Been stuck in a bed for over a year because of this.

  • @samkitty5894
    @samkitty5894 Před 11 měsíci +2

    How is GBS or it's cousin CIPD diagnosed? I have neuropathy below my waist that feels like GBS. I've seen army of doctors and specialists over the last 9 months. X-rays, CT scans, EKGs, MRIs, nerve conductivity studies, etc, etc. No diagnosis at all... So frustrating. Maybe they are hiding the dignosis due to my advanced age. GBS takes months even years to treat, and that costs money. I went from being 100% mobile to unable to walk. My legs feel like concrete blocks.

    • @DennisMC1974
      @DennisMC1974 Před 8 měsíci

      Me Too 😢

    • @samkitty5894
      @samkitty5894 Před 8 měsíci

      Sorry to hear. @@DennisMC1974

    • @shaiswei5626
      @shaiswei5626 Před 7 měsíci +1

      I was diagnosed with it almost a month ago they found out by doing a lumbar puncture.

    • @mizukimaiden
      @mizukimaiden Před 6 měsíci

      Lumbar puncture (added in combination with the other tests) is the only way to get a 100% confirmed diagnosis of GBS.
      ..Which also makes me feel as if many of these cases, (including this one!), actually got an incorrect diagnosis.
      They do want to get a patient SOME treatment in the meantime, since it truly isn’t known what is wrong at the current time.

  • @georgen9755
    @georgen9755 Před rokem

    I owe everything to Britannic , who made me so popular among my school days students and faculty , more particularly for the doctors were sympathetic to everyone at home , I especially recall Dr aggarwal specialises in tropical diseases, some skin rashes are so severe that you never know how it crops up and the medication were so good that after a regular course I got relieved of those rashes which appeared before sun rise and kept irritating until dawn , .

  • @RVS-pj6bd
    @RVS-pj6bd Před 5 měsíci +1

    I just had GBS last February of this year , 2024. Still recovering. I had 5 days of IVIG and able to walk now. My balance is still flaky and there are still pins and needles feeling on my palms and feet but I am determined to get through this. I had to take the Astra Zeneca vaccine to be able to work during the pandemic and it was required by the city government I live in. To put it simply, I had no choice. I am 53 and I wish I never took the vaccine but it is what it is. I wonder 20 years from now how Astra Zeneca will ever admit the side effects of its vaccine to the public. All written definitions of GBS says that it is a "rare" condition. After the pandemic, it is NOT rare anymore.

  • @Ook1731
    @Ook1731 Před rokem

    I got it from the mmr vaccine